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原发性血小板增多症中的铁储备。对26例患者的研究。

Iron stores in essential thrombocythaemia. A study of 26 patients.

作者信息

Cervantes F, Martí J M, López-Guillermo A, Piera C, Feliu E, Rozman C

机构信息

Postgraduate School of Haematology Farreras Valentí, University of Barcelona, Spain.

出版信息

Blut. 1989 Jun;58(6):291-4. doi: 10.1007/BF00320169.

Abstract

The iron status of 26 patients with essential thrombocythaemia (ET) was evaluated at diagnosis by means of bone marrow iron and blood studies, including serum ferritin determination. Nine patients were males, 17 females, and the mean age was 53 years (range 7-81). A decreased or absent iron level by semiquantitative estimation on bone marrow smears was observed in 77% of patients, and 81% had a low sideroblast score. Such a marrow pattern of iron depletion was equally distributed between both sexes. Contrasting with this, normal Hb, MCV, serum iron and serum ferritin were registered in the majority of cases. According to these results, absent or decreased marrow iron would be a common feature in ET, generally not reflecting true iron deficiency, as it occurs in the remaining chronic myeloproliferative disorders. Thus, in patients in whom ET is suspected, the diagnostic criterion of ruling out iron deficiency would be better served by serum ferritin measurement than by bone marrow iron estimation.

摘要

通过骨髓铁检查和血液研究(包括血清铁蛋白测定)对26例原发性血小板增多症(ET)患者在诊断时的铁状态进行了评估。9例为男性,17例为女性,平均年龄为53岁(范围7 - 81岁)。77%的患者骨髓涂片半定量估计显示铁水平降低或缺乏,81%的患者成红细胞铁粒幼细胞评分较低。这种骨髓铁耗竭模式在男女之间分布相同。与此形成对比的是,大多数病例的血红蛋白(Hb)、平均红细胞体积(MCV)、血清铁和血清铁蛋白均正常。根据这些结果,骨髓铁缺乏或减少是ET的常见特征,通常不反映真正的缺铁,正如在其他慢性骨髓增殖性疾病中所发生的那样。因此,对于疑似ET的患者,通过测定血清铁蛋白来排除缺铁的诊断标准比通过评估骨髓铁更好。

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